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Driven by an ever-expanding interest in new material systems with new functionality, the growth of atomic-scale electronic materials by molecular beam epitaxy (MBE) has evolved continuously since the 1950s. Here, a new MBE technique called hybrid-MBE (hMBE) is reviewed that has been proven a powerful approach for tackling the challenge of growing high-quality, multicomponent complex oxides, specifically the ABO3 perovskites. The goal of this work is to (1) discuss the development of hMBE in a historical context, (2) review the advantageous surface kinetics and chemistry that enable the selfregulated growth of ABO3 perovskites, (3) layout the key components and technical challenges associated with hMBE, (4) review the status of the field and the materials that have been successfully grown by hMBE which demonstrate its general applicability, and (5) discuss the future of hMBE in regards to technical innovations and expansion into new material classes, which are aimed at expanding into industrial realm and at tackling new scientific endeavors. [ABSTRACT FROM AUTHOR]

Double corundum-related polar magnets are promising materials for multiferroic and magnetoelectric applications in spintronics. However, their design and synthesis is a challenge, and magnetoelectric coupling has only been observed in Ni3TeO6 among the known double corundum compounds to date. Here we address the high-pressure synthesis of a new polar and antiferromagnetic corundum derivative Mn2MnWO6, which adopts the Ni3TeO6-type structure with low temperature first-order field-induced metamagnetic phase transitions (TN = 58 K) and high spontaneous polarization (~ 63.3 μC·cm-2). The magnetostrictionpolarization coupling in Mn2MnWO6 is evidenced by second harmonic generation effect, and corroborated by magnetic-field-dependent pyroresponse behavior, which together with the magnetic-field-dependent polarization and dielectric measurements, qualitatively indicate magnetoelectric coupling. Piezoresponse force microscopy imaging and spectroscopy studies on Mn2MnWO6 show switchable polarization, which motivates further exploration on magnetoelectric effect in single crystal/thin film specimens. [ABSTRACT FROM AUTHOR]

We report the observation of noncentrosymmetricity in the family of HRTiO4 (R = Eu, Gd, Dy) layered oxides possessing a Ruddlesden-Popper derivative structure, by second harmonic generation and synchrotron X-ray diffraction with the support of density functional theory calculations. These oxides were previously thought to possess inversion symmetry. Here, inversion symmetry is lifted by rotations of the oxygen-coordinated octahedra, a mechanism that is not active in simple perovskites. We observe a competition between rotations of the oxygen octahedra and sliding of a combined unit of perovskite-rocksalt-perovskite blocks at the proton layers. For the smaller rare earth ions, R = Eu, Gd, and Dy, which favor the octahedral rotations, noncentrosymmetricity is present but the sliding is absent. For the larger rare earth ions, R = Nd and Sm, the octahedral rotations are absent, but the sliding at the proton layers is present to optimize the length and direction of hydrogen bonding in the crystal structure. The study reveals a new mechanism for inducing noncentrosymmetricity in layered oxides, and chemical-structural effects related to rare earth ion size and hydrogen bonding that can turn this mechanism on and off. We construct a phase diagram of temperature versus rare earth ionic radius for the HRTiO4 family. [ABSTRACT FROM AUTHOR]

ABSTRACT Linear electrogyration (electric field-induced optical activity) and electro-optic effects in x-cut and z-cut right-handed (RH) α-quartz were measured using a complete Mueller matrix polarimeter. The polarimeter used in the analysis was equipped with four photoelastic modulators operating at different frequencies. This configuration is especially sensitive due to the fidelity of the modulators and the fact that all the Mueller matrix elements can be delivered without any moving . The linear electrogyration coefficient γ11 as a function of the wavelength of incident light was remeasured. The coefficient γ33, required by symmetry to be zero, was evaluated as a control. γ11 was much smaller than values obtained previously using devices dependent on mechanical light modulation. Electrogyration measurements have often been confounded by the much larger linear electro-optic effect. The Mueller calculus used herein is well suited to the separation of the competing changes to the polarization state of light. Quadratic electrogyration associated with elements β11 and β33 was not detectable. Chirality 26:70-73, 2013. © 2013 Wiley Periodicals, Inc. [ABSTRACT FROM AUTHOR]

Over the past few years, several studies have reported the existence of polar phases in n = 2 Ruddlesden-Popper layer perovskites by trilinear coupling of oxygen octahedral rotations (OOR) and polar distortions, a phenomenon termed as hybrid improper ferroelectricity. This phenomenon has opened an avenue to expand the available compositions of ferroelectric and piezoelectric layered oxides. In this study, we report a new polar n = 2 Ruddlesden-Popper layered niobate, Li 2 SrNb 2 O 7 , which undergoes a structural transformation to an antipolar phase when cooled to 90 K. This structural transition results from a change in the phase of rotation of the octahedral layers within the perovskite slabs across the interlayers. First-principles calculations predicted that the antipolar Pnam phase would compete with the polar A 2 1 a m phase and that both would be energetically lower than the previously assigned centrosymmetric Amam phase. This phase transition was experimentally observed by a combination of synchrotron X-ray diffraction, powder neutron diffraction, and electrical and nonlinear optical characterization techniques. The competition between symmetry breaking to yield polar layer perovskites and hybrid improper antiferroelectrics provides new insight into the rational design of antiferroelectric materials that can have applications as electrostatic capacitors for energy storage., Competing Interests: The authors declare no competing financial interest.

The group VIb dichalcogenides (MX 2 , M = Mo, W; X= S, Se) have a layered molybdenite structure in which M atoms are coordinated by a trigonal prism of X atoms. Ternary solid solutions of MS x Se 2- x were synthesized, microcrystals were grown by chemical vapor transport, and their morphologies and structures were characterized by using synchrotron X-ray diffraction, Rietveld refinement, DIFFaX simulation of structural disorder, scanning electron microscopy, and energy dispersive X-ray spectroscopy. Double aberration corrected scanning transmission electron microscopy was used to determine the anion distributions in single-layer nanosheets exfoliated from the microcrystals. These experiments indicate that the size difference between S and Se atoms does not result in phase separation, consistent with earlier studies of MX 2 monolayer sheets grown by chemical vapor deposition. However, stacking faults occur in microcrystals along the layering axis, particularly in sulfur-rich compositions of MS x Se 2- x solid solutions., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)